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36199

Tridemorph

PESTANAL®, analytical standard

Synonym(s):

2,6-Dimethyl-4-tridecylmorpholine

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About This Item

Empirical Formula (Hill Notation):
C19H39NO
CAS Number:
24602-86-6
Molecular Weight:
297.52
NACRES:
NA.24
PubChem Substance ID:
329755340
UNSPSC Code:
41116107
EC Number:
246-347-3
MDL number:
MFCD00055522
Technical Service
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grade

analytical standard

Quality Level

100

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

application(s)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

SMILES string

CCCCCCCCCCCCCN1CC(C)OC(C)C1

InChI

1S/C19H39NO/c1-4-5-6-7-8-9-10-11-12-13-14-15-20-16-18(2)21-19(3)17-20/h18-19H,4-17H2,1-3H3

InChI key

YTOPFCCWCSOHFV-UHFFFAOYSA-N

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

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Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Repr. 1B - Skin Irrit. 2

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

农药列管产品

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Certificates of Analysis (COA)

Lot/Batch Number
BCBW9105

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S Silve et al.
Biochimica et biophysica acta, 1392(2-3), 233-244 (1998-06-19)
Lamin B receptor (LBR), a nuclear protein of avian and mammalian cells, contains an hydrophobic domain that shares extensive structural similarities with the members of the sterol reductase family. To test if the sterol-reductase-like domain of LBR could be enzymatically
Xia Tian et al.
The Journal of organic chemistry, 71(8), 3176-3183 (2006-04-08)
Tandem Prins cyclization and Friedel-Crafts reaction with an electron-rich aromatic ring were used to prepare the core structures of calyxin natural products. The proposed structure of epicalyxin F was prepared and shown to be incorrect. Several calyxin natural products, including
D Raederstorff et al.
European journal of biochemistry, 164(2), 427-434 (1987-04-15)
The sterols and sterol precursors of two amoebae of the genus Naegleria, Naegleria lovaniensis and Naegleria gruberi were investigated. Cycloartenol, the sterol precursor in photosynthetic organisms, is present in both amoebae. In N. lovaniesis, it is accompanied by lanosterol and
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Global Trade Item Number

SKUGTIN
36199-100MG04061831824674